anomalous trichromacy

human disease

Facts

3 properties
Instance of
class of disease
Subclass of
color vision, congenital color blindness, dyschromatopsia, partial color blindness
Studied by
biology of colour[6]
🏷️ Also known as
en anomalous trichromatism en partial colour blindness en Color anomaly en anomalous trichromacy da anomal trikromasi de anomale Trichromasie de anomaler Trichromatismus fr trichromatie anormale ja 異常3色覚 ru аномальная трихромазия
🔖 Identifiers · 5
Google Knowledge Graph ID
/g/11gfhx1c3b
Human Phenotype Ontology ID
HP:0011519
IEV number
845-22-035
UMLS CUI
C4023316

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Summary

anomalous trichromacy is a class of disease[1]. It is a type of color vision[2], congenital color blindness[3], dyschromatopsia[4], and partial color blindness[5].

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). anomalous trichromacy. Retrieved November 4, 2026, from https://4ort.xyz/entity/anomalous-trichromacy
MLA “anomalous trichromacy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/anomalous-trichromacy.
BibTeX @misc{4ortxyz_anomalous-trichromacy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{anomalous trichromacy}}, year = {2026}, url = {https://4ort.xyz/entity/anomalous-trichromacy}, note = {Accessed: 2026-11-04}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): anomalous trichromacy — https://4ort.xyz/entity/anomalous-trichromacy (retrieved 2026-11-04)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 18w ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗
    Studied by → biology of colour
    UMLS CUI → C4023316
    Human Phenotype Ontology ID → HP:0011519
    Google Knowledge Graph ID → /g/11gfhx1c3b
    + 5 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39873: P31 = "type of disease""
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.